Oxidation resistant polymeric compositions prepared from 3 - n-(4&#39; - anilinophenyl)amino - 2-hydroxypropyl methacrylate

ABSTRACT

ANTIOXIDANTS UCH AS THE REACTION PROODUCT OF P-AMINODIPHENYLAMINE AND GLYCIDYL METHACRYLATE (3-N-(4&#39;&#39;-ANILINOPHENYL) AMINO-2-HYDROXYPROPYL METHACRYLATE), AND THE REACTION PRODUCT OF N-HEXYL-N&#39;&#39;- PHENYL-P-PHENYLENEDIAMINE AND GLYCIDYL METHACRYLATE (3-(N-(4&#39;&#39;-AMINILINOPHENYL)-N(1,3-DIMETHYLBUTYL) AMINO-2-HYDROXYPROPYL METHACRYLATE), AGE RESISTANT POLYMERS HAVING MONOMERIC AGE RESISTERS PHYSICALLY COMBINED THEREWITH AND OXIDATION RESISTANT POLYMERI COMPOSITIONS PREPARED BY FREE RADICAL POLYMERIZATION TECHNIQUES INVOLVING THE USE OF SAID ANTIOXIDANTS AS MONOMERS.

UnitedStates Patent Oflice 3,817,916 Patented June 18, 1974 ABSTRACT OF THE DISCLOSURE Antioxidants such as the reaction product of p-aminodiphenylamine and glycidyl methacrylate [3-N-(4'-anilinophenyl)amino-Z-hydroxypropyl methacrylate], and the reaction product of n-hexyl-N'-phenyl-p-phenylenediamine and glycidyl methacrylate [3-[N-(4'-anilinophenyl)-N- (1,3 dimethylbutyl)]amino-2-hydroxypropyl methacrylate], age resistant polymers having monomeric age rcsisters physically combined therewith and oxidation resistant polymeric compositions prepared by free radical polymerization techniques involving the use of said antioxidants as monomers.

This invention relates to monomeric antioxidants, oxidation resistant polymeric compositions and processes for preparing said monomeric antioxidants and oxidation resistant compositions. More particularly, the invention relates to a process of preparing polymeric compositions containing antioxidants which are not susceptible to solvent extraction and which are resistant to volatilization.

Essentially all types of rubber, both natural and synthetic, and particularly rubbers formed from dienes, are known to be susceptible to deterioration resulting from prolonged exposure to oxidative aging. A great deal of effort has been expended by those engaged in the field of polymer technology to develop various stabilizers that will effectively inhibit the adverse effects of aging of polymeric compositions. Unfortunately, many of the commercially accepted stabilizers may be volatilized when the polymeric products are exposed to elevated temperatures and/ or high vacuum over prolonged periods of time. Furthermore, they are rather quickly extracted from polymeric compositions by repeated washings with aqueous detergent solutions or organic solvents. These severe conditions are routinely encountered by garments containing latex treated fabric when they are subjected to frequent laundering or dry-cleaning.

It is, therefore, an object of this invention to provide a process for preparing oxidation resistant polymeric compositions. A further object of this invention is to provide a process of preparing polymeric compositions that are highly resistant to oxidative aging at elevated temperatures even after repeated exposure to aqueous detergent solutions or dry-cleaning fluids. It is a still further object of this invention to provide a process of preparing polymers possessing antioxidants chemically bound thereto.

In accordance with the present invention oxidation resistant polymeric compositions are prepared by polymerizing a monomeric amine antioxidant with one or more cornonomers.

The amine antioxidants of the present invention have the following structural formula.

- wherein R is selected from the group consisting of alkyl radicals having 1 to 12, preferably 3 to 12, carbon atoms, cycloal-kyl radicals having 5 to 12 carbon atoms, aralkyl radicals having 7 to 24 carbon atoms and aryl radicals having 6 to 24 carbon atoms wherein R and R are selected from the group consisting of hydrogen and alkyl groups having 1 to 4 carbon atoms and wherein R is selected from the group consisting of hydrogen, alkyl radi cals having 1 to 12 (preferably 1 to 8) carbon atoms, cycloal-kyl radicals having from 5 to 12 carbon atoms, and aralkyl radicals having 7 to 24 carbon atoms, preferably a benzyl or a-phenethyl radical wherein R R R, R", and R are selected from the group consisting of hydrogen and alkyl radicals having from 1 to 4 carbon atoms, i.e. methyl, ethyl, propyl, and butyl radicals, the sum of the carbon atoms in R and R preferably being 4 or less, and the sum of carbon atoms in R and -R preferably being 4 or less; wherein R is selected from the group consisting of hydrogen; alkyl radicals having from 1 to 4 carbon atoms, i.e., methyl, ethyl, propyl, and butyl radicals; carboxymethyl radical and carbalkoxymethyl radicals; and wherein R is selected from the group consisting of hydrogen; alkyl radicals having from 1 to 4 carbon atoms, i.e., methyl, ethyl, propyl, and butyl radicals; phenyl and substituted phenyl radicals, e.g., a phenyl group having located in the para position, an alkyl radical having 1 to 4 carbon atoms such as methyl, or an alkoxy radical having 1 or 2 carbon atoms, e.g., methoxy; carboxyl radical and carbalkoxy radicals.

Preferably -NHR is in the para position. Under structural formula (I), the carbalkoxymethyl radicals preferably have the following structural formula:

-cmc-o-R wherein R is an alkyl radical having from 1 to 4 carbon atoms. The carbalkoxy radicals preferably have the fol lowing structural formula:

3'-( -anilino amlinof f-hydroxypropylmetlracrylate 3'-N-(4"-anilinophenyl)amino-2'-hydroxy-1'-methylpropyl methacrylate 3 '-N- (4"-anilinophenyl) amino-2'-hydroxy-1',2',3

trimethylpropyl methacrylate 3 '-N- (4"-ani1inopheny1) amino-2-hydroxy- 1 ',1'-di-nbutylpropyl methacrylate 3-N-(4"-anilinophenyl)aming- '-hydroxypr0pyl acrylate '-N- 4"-anilinophenyl) amino-2'-hydroxypropyl-2- methoxy methacrylate H 1 3 '-N- (4"'-anilinoph'enyl) amino-2' hydroxypropylf2f carboxy methacrylate 3'-N-(4"-anilinophenyl)amino-2-hydroxypropyl-3- phenyl methacrylate 3 '-N- (4"-anilinophenyl) amino-2'-hydroxypropyl-3- methoxy methacrylate 3'-N-( "-anilinophenyl)amino-2'-hydroxypropyl-3- (4-carboxy phenyl) methacrylate 3'-N-(4"-anilinophenyl)amino-2'-hydroxypropyl-3- (4-carbmethoxy phenyl) methacrylate 3'-N-(4"-anilinophenyl)-N-isopropyIamino-2'-hydroxypropyl methacrylate 3'-N-(4"-anilino-3"-methylphenyl)amino-2'-hydroxypropyl methacrylate 3 -N-( 4"-anilino-3 "-cyano ethylphenyl) amin-2-hydroxypropyl methacrylate -(4"-anilino-2"-tolylpheny1)amino-2'-hydroxypropyl methacrylate '-N- 4"-anilino-2"-cyc1ohexylphenyl) amino-2'- hydroxypropyl methacrylate 3'-N-(4"-anilino- "-benzylphenyl) amino-2'-hydroxypropyl methacrylate '-N-[4"-(2"-mcthylanilino)phenyl]amino-2-hydroxypropyl methacrylate 3'-N-[4"-(2"-cyanomethylanilino)phenyl]amino-2'- hydroxypropyl methacrylate '-N-[4"-(2"-tolylanilino)phenyl]amino-2'-hydroxypropyl methacrylate 3 '-N- [4"- (4"-cyclohexylanilino) phenyl] amino-2'- hydroxypropyl methacrylate 3 -N- [4' '-benzylanilino phenyl] -2'-hydroxypropyl methacrylate When polymerized, the amine antioxidants of the present invention form segmers having the following structural formula.

5:0 11 47-11 ra e-0H The monomeric antioxidants can easily be prepared by dissolving the aforementioned amines in a solvent such a's-be'nz'ene, adding a phenol or phenolate catalystg s'uch as sodium or potassium phenolate, and then slowlyadding the epoxy compound. Preferably the reac't'ioncomposir tion is heated and stirred-for several hours, for examp1e'at 50 C." to 60 C. for 2 hours. Thesolvntis-thenremoved, e.g., by a rot'ary evaporatorfl i -Tl1e' amine'ag'e' resisters which are used: within the practice of the preseut'invention "can be 'prepared"'by reacting (A) at least one amine compound as described a N-1 methylheptyl-N' pphenylenediamine' 'hereinafter'witlr at least one epoxy compoundhaving thefollowing structural formula:

Representative epoxy compounds which can be used to prepare the monomeric age resisters of the present invention are: p

The epoxy compounds can be prepared by the reaction of epichlorohydrin with a carboxylic acid in the presence ofabase. j

The amine compounds which gfa'n'b'e reactedjwithftlie aforementioned epoxyjcompoun'ds to prepare the amine age resisters of the present invention contorm to the: following structural formula.

In preparing the amine antioxidants of thepre'sent invention, consideration should lie-given to'the'activit'ies of the R--NH- and R NH'" groups" with epoxy groups. If one amine-group'- is more reactive with epoxy groups than the other amine group, "there is a greater possibility that the amine reactant will react 'with 'one, rather than two epoxy groups; The activity of the amine groups is dependent upon the nature of the R and R radicals. Normally amine groups possessing alkyl or aralkyl substituents aremore reactive than amine"groups containing aryl substituents. Amine'groups-possessing large substituents are generally less'reactive with epoxy groups than amine groups containing smaller substituents:

Representative amine compounds'which can'be used to prepare the monomeric age resisters of the present inventtionare: Y. an.

N,N'-dimethyl-p-phenylenediarnine' A 5 N,N'-di-beta-naphthyl-p phenylenedianiine' N,N'-bis( 1-ethyl-3-methylpentyl) p-phenylenediamine N,N-bis(l-methylheptyl')-P'PhenYlenediamine' N,N'-bis(sec.butyl)-p pheny1enediamine t N-phenyl-N'-beta-hydroxylethyl-p-phenylenediami 1- Nphenyl-N-cyanoethyl-p-phenylenediamine N-sec.butyl N?-cyanoethyl-p-phenylenediamine I v '1 1' N;beta-naphthyl-Nt-sec,butyl-p phenylenediamine N,Nf-diphenethyl-paphenylenediamine N-me thyl-N'-phenyl-p-phenylenediamine v N-ethyhN'ephenyl-pphenylenediamine a f N-isopropyl-N-phenyl-p-phenylnediami fi N-sec;butyl-N'-phenyLp-phenyIeriediaEnine N-cyclohexyI-N'-phenyl p-phenylenediamine f I I N-1,3-dimethylbutyl N-phenyl-p phenylenediami -N-phenethyl-N' phenyl-p-phenylenediamine N-benzyl-N'-phenyl-p-phenylenediamine i A particularly representative amine is p-aminodiphenylamine.

Para-aminodiphenylamine and the rest of the amine compounds whichcan be used to prepare the monomeric antioxidants of the present invention are known in the prior art and can be prepared by well known prior art methods.v U.S. 2,381,015; U.S. 3,209,030 and British Pat. 1,064,958il1ustrate some prior art methods.

The-aforementioned monomeric antioxidants may be polymerizedby well known free radical polymerization techniques with oneor more comonomers that are known to polymerize in free radical initiated polymerization systems. The polymerization may be carried out in emulsion, suspension, bulk'or solution type systems. Some adjustments in the polymerization recipe and/or conditions may be necessary to obtain a satisfactory rate of polymer formation, depending on the amount of monomeric antioxidant included and the other monomers involved. Adjustments which may be necessary in the polymerization conditions to improve polymerization rates include increasing the temperature of polymerization and/or increasing the initiator level and/or increasing thelevel-of activator ingredients. Solvents may also be required to obtain adequate solubility of the monomers with each other as well as to solubilize other ingredients where required. Some solvents, such as methyl ethyl ketone or isopropyl alcohol, can be used to advantage with an emulsion polymerization system. These adjustments, where necessary, are to counteract the inhibitory effect ofthe monomeric antioxidant and to insure its solubility in the system.

Examples of free radical initiators that are useful in :the practice of this invention are those known as Redox initiators, such as appropriate combinations of chelated iron salts, sodium formaldehyde sulfoxylate and organic hydroperoxides such as cumene and paramenthane hydroperoxides. Other initiators such as azoisobutyronitrile, benzoyl peroxide, hydrogen peroxide and potassium persulfate may also be used, depending on the particular polymerization system.

The special monomers used in the practice of this invention have certain chemical characteristics which preclude their use in polymerization processes other than those initiated by free radicals. By free radical initiated systems is meant systems wherein free radicals are generated by any of various processes such as thermal decomposition of various persulfate, perborate, peroxide, azo or azonitrile compounds; induced (catalytic or Redox promoted) decomposition of various persulfate, peroxide or hydroperoxide compounds and generation of free radicals by exposure of the system to high energy radiation such as radiation from a radioactive source or ultraviolet light. Such-systems are very well known in the art and are widely used commerically, e.g., in the preparation of SBR, styrene/butadiene copolymers.

The" 1most widely used system for preparation of elastomeric polymers,i.e., polymers prepared from a monomer charge made up of at least 40 percent diene, preferably at least 60 percent diene, by free radical initiation is the emulsion system. Polymers ranging all the way from liquid, low molecular'weight (mol wts. of about 1,000 to 5,000) to polymers of intermediate molecular weight (60,000 to 70,000 and higher) to oil extendable, at least 50'percent soluble, rubbery solid, high molecular weight (100,000 to 500,000 or more) and even highly gelled, less than 50 percent soluble, may be prepared by emulsion polymerization. The monomeric age resisters of the present invention can be used in such emulsion polymerization systems to produce polymers of the aforementioned yp The principles of emulsion polymerization are discussed in references such as Synthetic Rubber by G. S. Whitby, Editor-in-Chief, John Wiley and Sons, 1954, particularly Chapter 8, and Emulsion Polymerization by F. A.

1 Number average molecular weights.

Bovey et al., Vol. IX of High Polymers, Interscience Publishers Inc. 1955. Some specialized applications of 1 these principles are indicated in U.S. Pats. such as 3,080,-

334; 3,222,334; 3,223,663; 3,468,833 and 3,099,650.

Very effective as free radical polymerization initiators used within the practice of the present invention, when form very effectively when used in polymerization recipes containing appropriate levels of supporting ingredients. By supporting ingredients is meant those materials often referred to as activators in emulsion, or other systems, where required. U.S. Pat. No. 3,080,334 describes some of these materials at column 5, lines 20-26. Such materials can also be referred to as catalyst activators. The term Redox Polymerization is often used where the complete initiation system includes a Redox system, i.e., reducing agents and oxidizing agents in a proportion that yields polymerization initiating species. All of these initiator systems are well known in the art.

Emulsion and suspension polymerizations are normally accomplished in the range of 5 C. to C. while the temperature range for solution or bulk polymerizations is normally 20 C. to C. Though the activated or Redox initiated systems are preferred for low temperature polymerizations, they are very effective at high temperatures also, normally requiring appreciably lower quantities of the various ingredients to obtain a desirable polymerization rate.

The free radical sources used in the initiator systems are those customarily used in free radical polymerizations, for example, organic initiators such as azo-nitriles, azoderivatives, peroxides, and hydroperoxides and inorganic initiators such as inorganic peroxy compounds. Radiation, e.g., of the ultra-violet and gamma type can also be used as a free radical source. Various organic initiators are described by I. Brankrup and E. H. lmmergut, Polymer Handbook (John Wiley & Sons), 1965, pages 11-3 to 11-51. Peroxide initiators include the aralkyl, aliphatic, aliphatic acyl, aromatic acyl, ketone, aldehyde and perester types. Hydroperoxide compounds include aralkyl and aliphatic hydroperoxides. Inorganic peroxy compounds include persulfates, perborates, perphosphates and hydrogen peroxide.

Arakyl peroxides are represented by dicumyl peroxide; aliphatic peroxides by di tert.butyl peroxide; aliphatic acyl peroxides by acetyl peroxide, decanoyl peroxide and lauroyl peroxide; aromatic acyl peroxides by benzoyl peroxide and 2,4-dichlorobenzoyl peroxide; ketone peroxides by methylethyl ketone peroxide and cyclohexanone peroxide; aldehyde peroxides by heptaldehyde peroxide; and perester peroxides by tert.butyl peracetate, tert.butyl perpivalate and tert.butyl perbenzoate. Aralkyl hydroperoxides are represented by cumene hydroperoxide and diisopropylbenzene hydroperoxide and aliphatic hydroperoxides by tert.butyl hydroperoxide and paramenthane hydroperoxide. Persulfate, perborate and perphosphate compounds are represented by the sodium, potassium and ammonium persulfates, perborates and perphosphates; azonitriles and azo-derivatives by 2,2-azo-bis-isobutyronitrile, 2,2-azo-bis-2-methylpropionitrile and azo-bis-diphenylmethane.

Supporting ingredients, i.e., activators capable of activating certain initiators to produce free radicals include iron compounds such as ferrous sulfate or cobalt compounds, complexed with compounds such as sodium salts of ethylene diamine tetra acetic acid or sodium or potassium pyrophosphate. Reducing agents used in Redox systems include sodium formaldehydesulfoxylate, various sugars and hydrosulfites.

Various initiator system components are described at column 4, lines 14 to 32, in U.S. Pat. No. 3,080,334.

Examples of comonomers that are useful in the practice of this invention in combination with the monomeric antioxidants are polymerizable unsaturated hydrocarbons, both substituted and unsubstituted, including conjugated diene monomers, such as butadiene-1,3; 2 -chlorobutadicue-1,3; isoprene; 2-ethyl butadiene-l,3; piperylene; and hexadienes and copolymerizable monoolefins including vinyl and vinylidene monomers such as styrene, tic-methylstyrene, divinyl benzene, vinyl chloride, vinyl acetate, vinylidene chloride, methylmethacrylate, ethylacrylate, the vinylpyridines including 2-vinyl pyridine, S-methyl- Z-vinylpyridine, 4-vinyl pyridine and 2-vinyl-5-ethyl pyridine, acrylon itrile, methacrylonitrile, methacrylic acid and acrylic acid. Mixtures of the monomeric antioxidants and mixtures of the comonomers may be used. The monomer charge weight ratio is normally from about 0.10/ 99.9 to about 10/90 or even 20/80 monomeric antioxidant/comonomer. The ratio may even be as high as 30/70 or 60/ 40. A charge ratio of about 0.5/99.5 to about 5.0/95 is preferred. Ratios will vary depending on the amount of antioxidant desired to be bound and on the reactivity ratios of the monomers in the particular polymerization system used. However, the ratio may be even higher and the monomeric antioxidant may even constitute all of the monomer charged, i.e., the ratio can be 100/0.

Preferably the monomer system contains at least 50 parts by weight per 100 parts by weight of total monomer of at least one diene, preferably a conjugated diene, such as 1,3-butadiene or isoprene. It always contains at least 40 parts by weight of said diene.

One embodiment of the present invention involves the use of a monomer system comprised of from about 50 to about 99.9 parts of at least one diene monomer, preferably a conjugated diene, to about 49.9 parts of at least one monomer selected from the group consisting of vinyl monomers and vinylidene monomers and from about 0.10 to 5.0 parts by weight of atleast one monomeric antioxidant, all parts being parts by weight per 100 parts by weight of total monomer. Preferably at least 0.5 part of monomeric antioxidant is used. When at least 0.5 part of the monomeric antioxidant is used, the upper limit on the diene monomer range is 99.5 parts and the upper limit of the vinyl monomer and/or vinylidene monomer range is 49.5 parts. The upper limit of the monomeric antioxidant range may be even higher than 5.0, i.e., 10, 20, 30 and even 50.

The polymers resulting from the free radical polymerizations of monomeric systems containing the monomeric antioxidants of the present invention have a special advantage in that the age resistant portion is not extractable, and therefore the polymeric compositions are highly resistant to oxidative aging even after repeated exposure to aqueous detergent solutions or dry-cleaning fluids. This feature is especially significant where polymers are used in foam backings for rugs and where polymers are used in solution or latex form to treat fabrics, since such products are often exposed to aqueous detergent solutions or dry-cleaning fluids. This feature is also significant where factors such as contact with lubricating oils or exposure to high vacuum conditions are a consideration.

One of the advantages of the present process is that it permits the preparation of polymers preparedfrom monomers systems containing diene monomers and containing built-in stabilizers, without the formation of appreciable gel, that is, polymers can be made which are essentially gel-free. Gel formation is generally undesirable in a polymer since it can cause processing difficulties and directly and/or indirectly can affect the physical properties of the polymer in its vulcanized form. Normally a macro gel content of less than 50 percent is desirable. Preferably a gel content of less than 10 percent is desirable. Most preferably a gel content below 5 percent is desirable. Gel is the amount of polymer that is insoluble in an organic solvent such as benzene. One way to measure gel content comprises placing about 0.20 to about 0.30 grams of the polymer in 100 milliliters of benzene and permitting the mixture to stand for 48 hours.

The mixture is then'filtered through a l00inesh stainless steeliwire cloth having a wire diameter of 0.045 inch solids is. then run on the filtrateto determinethe amount of soluble polymer. The-amount of gel the: difference between the amountof polymer placed infthe, benzene originally and the amount of soluble polymer. The percent gel is one hundred times the gel weight divided by the original polymer weight. p To aflord adequate protection against degradation the polymers should contain from about 0.10 part to about 10.0 parts by weight of the segmeric form of the monomeric antioxidant per parts by weight of thepoIy; mer, although from about 0.50 partpto about 5.0 parts is normally satisfactory, from about 0.50 Part to about 3.0 parts being preferred. As much as 20 parts, 30 parts, 50 parts and more of the polymer may consist of theantioxidant segmeric unit while the lower limit may bej part to 0.10 part and lower. In fact, polymers containing 100 percent antioxidant segmeric units may be, produced, if desired. However, as the amount of bound antioxidant increases the physical characteristics of the polymer are altered accordingly. Where itis desired to producea polymer which is self stabilizing and which substantially retains the physical properties of the comonomer or c0. monomers, normally the polymer should contain no more than about 10.0 parts by weight of theantioxidant egmeric unit, i.e., repeat unit. Such polymers preferably are solid, although they may be liquid. Where it is desired that the polymer act as a polymeric antioxidant which may be blended with unstabilized polymers the: polymer should normally contain greater amounts" of'the monomeric antioxidant. The remainder of thepol'ymer'is comprised preferably of the segmeric forrn of at least one conjugated diene monomer and/orthe segmeric form of at least one vinyl monomer. Preferably the polymers contain at least 50 percent by weight of the segmeric form of a diene, preferably a conjugated diene such as butadiene-1,3 or isoprene. Most preferred are polymers containing from about 50 to about 99.9 parts by weight of the segmeric form of at least one diene,'preferably a conjugated diene, 0 to about 49.9 parts byweightof the segmeric form of at least one monomer selected from the group consisting of vinyl monomers and vinylidene monomers and 0.10 to 5.0 parts by weight ofthe segmeric form of at least one monomeric antioxidant, all partsbeing by weight per 100 parts by weight of polymer. Preferably the polymer contains at least'0.5 part of the segmeric form of the monomeric'antioxidant. When the polymer contains at least 0.5 part of thesegmeric form of the monomeric antioxidant, the upper limitof dienesegmer range is 99.5 parts and the upper limit of the vinylsegmer and/ or vinylidene segmer range is 49.5 parts. The upper limit of the segmeric form of the monomeric antioxidant range may be even higher than 5.0, i.e., 10, 20, 30 andeven 50. In all instances the polymers must contain at least 40 parts by weight of the segmeric form ofa diene monomer, preferably a conjugated diene. In polymers generally prepared by free radical, particularly emulsion techniques, the trans-1,4 content is generally greater'than the cis-l,4 or 1,2 content. i j All of the monomeric amine antioxidants described herein are capable of stabilizing polymer's'by' simple incorporation into the polymers by conventional techniques such as by addition to polymer latices or by addition to the solid polymer on a mill or in aBanbury. When blending a self-stabilizing polymer with other polymers, es pecially when the self-stabilizing polymer'contains large amounts of the segmeric form of the monomeric antioxidant, one must consider the solubility problems involved in blending dissimilar polymers. x

Polymers subject to deterioration by oxidationthatcan be conveniently protected by the antioxidants described herein include substituted and unsubstituted, saturatedand unsaturated, natural and synthetic polymers. Theoxidizable natural polymers include natural rubber in its various forms, e.g., pale crepe and smoked sheet, and balata and gutta percha. The oxidizable synthetic polymers are prepared from a single monomer (homopolymer) or a mixture of two or more copolymerizable monomers (copolymers) wherein themonomers are combined in a random distribution or block form. The monomers may be substituted or unsubstituted and may possess one or more double bonds, for example, diene monomers, both conjugated and nonconjugated, and monoolefins including cyclic and acyclic monoolefins, especially'vinyl and vinylidene monomers. Examples of conjugated dienes are 1,3- butadiene, isoprene, chloroprene, 2-ethyl-1,3-butadiene, 2, 3 dimethyl-1,3-butadiene and piperylene. Examples of nonconjugated dienes are 1,4-pentadiene, 1,4-hexadiene, 1,5-hexadiene, dicyclopentadiene, 1,5-cyclooctadiene and ethylidene norbornene. Examples of acyclic monoolefins are ethylene, propylene, l-butene, isobutylene, l-pentene and l-hexene. Examples of cyclic monoolefins are cyclopentene, cyclohexene, cycloheptene, cyclooctene and 4- methyl-cyclooctene. Examples of vinyl monomers are styrene acrylonitrile, acrylic acid, ethylacrylate, butylacrylate, methyl vinyl ether, vinyl acetate and vinyl pyridine. Examples of vinylidene monomers are a-methylstyrene, methacrylic acid, methyl methacrylate, ethyl methacrylate, glycidyl methacrylate and vinylidene chloride. Representative examples of the synthetic polymers used in the practice of this invention are polychloroprene; homopolymers of a conjugated 1,3-diene such as isoprene and butadiene, and in particular, polyisoprenes and polybutadienes having essentially all of their repeat units combined in a cis-l,4 structure; copolymers of a conjugated 1,3-diene such as isoprene and butadiene with up to 50 percent by weight of at least one copolymerizable monomers including ethylenically unsaturated monomers such as styrene or acrylonitrile; butyl rubber, which is a polymerization product of a major proportion of a monoolefin and a minor proportion of a multiolefin such as butadiene or isoprene; polyurethanes containing carbon to carbon double bonds; and polymers and copolymers of monoolefins containing little or no unsaturation, such as polyeth ylene, polypropylene, ethylene propylene copolymers and terpolymers of ethylene, propylene and a nonconjugated diene such as dicyclopentadiene, 1,4-hexadiene, ethylidene norbornene and methylene norbornene.

When added in free form normally 0.001 to 10.0 percent of the antioxidant by weight, i.e., parts by weight based on the weight of the polymer, i.e., 100 parts by weight of the polymer can be used, although the precise amount of the antioxidant which is to be employed will depend somewhat on the nature of the polymer and the severity of the deteriorating conditions to which the polymer is to be exposed. In unsaturated polymers such as those made from conjugated dienes, the amount of antioxidant necessary is greater than that required by a saturated polymer such as polyethylene. It has been found that an effective antioxidant amount of the disclosed stabilizers in rubbery unsaturated polymers will generally range from 0.05 to 5.0 percent by weight i.e., parts by weight based on the weight of the polymer, although it is commonly preferred to use from 0.5 to 3.0 percent by weight, i.e., parts by weight based on the weight of the polymer. Mixtures of the antioxidants may be used.

The following examples illustrate the practice of the present invention. Unless otherwise indicated, all parts are parts by weight.

Example 1 Para-aminodiphenylamine (62.5 grams/0.34 mole) was dissolved in 670 ml. of benzene. The catalyst was prepared by adding one gram of sodium hydroxide and one gram of phenol to 5 ml. of water. Five milliliters of ethanol was added to insure solubility in the benzene. After adding the catalyst, 24 grams (0.169 mole) of glycidyl methacrylate was added slowly from a dropping funnel and the mixture was stirred for 18 hours at room temperature. The solvent was then removed with a 10 rotary evaporator. The yield was 55 grams (93%). melting point of the product was 126 C.

Example 2 I I Ninety-one grams (0.34 mole) of l l-1,3-dimethylbutyl- N'-phenyl-phenylenediamine were dissolved in 670 milliliters of benzene. Catalyst was prepared and glycidyl methacrylate was added as described above. The yield Examples 3 to 7 The following polymerizations were carried out using the following recipes.

TABLE I Order Examples (parts) oi addition Ingredients 3 4 5 6 7 'Water 194 200 194 195 195 Potassium soap of disproportionated rosin acids.;- 2. 8 2. 7 2. 7 2. 7 2. 7 Sodium soap of tallow fatty 1 acids 2 4 2. 4 Tiisodium phosphate. 375 Sodium hydrosulfite.- 009 Sodium salt of condensed naphthalene sulionic acid..-.' 08 08 15 08 08 Tripotassium phosphate 25 "Styrene 20 20 20 20 9 Acrylnnitrilp 30 Tertiary dodecyl mercaptan.-. 25 60 30 40 30 Monomeric antioxidant .a 1.25 1.25 5.0 1.25 1.25 3 .{Methyl ethyl ketone 55 55 55 44 Cynlnhmrmmna 45 4 Butadiene-1,3 75 67 75 75 75 ater 5 11 5 11 11 Chelating agent .077 .038 .077 .038 .023 5 Ferrous sulfate heptahydrate. 02 0075 02 009 02 Sodium formaldehyde sulfoxylate 04 10 02 08 05 Sodium hydrosulfi 01 002 004 Styrene 2. 4 2. 4 6 Aerylnnitrila arameuthane hydroperoxide- .04 05 .02 .02 .01

Polymerization temperature F.) 41 77 45 70 122 Polymerization time (hours) 13 19 10 10 12 Percent conversion 65 79 65 66 00 1 Approximately 1/1 (molar ratio) reaction roduct oi glycidyl methaerylate and p-amlnodiphenylamiue, the ma or component being 3-N (4-anihnophe1 1yl)amino-2-hydroxypropyl methacrylate. The antioxidant alas distsolved 1n 3.5!. parts of methyl ethyl ketone before being added to e sys em.

2 /10 mixture of tetrasodium salt of ethylene diamine tetra-acetic acid and monosodium salt of N,N-di(a.-hydroxyethyl) glycine.

The above polymerization systems were shortstopped with 0.10 part of sodium dimethyldithiocarbamate and 0.05 part of diethylhydroxylamine in 4.4 parts of water. A very small amount of sulfuric acid was added to at least one number 5 solutions to dissolve any ferrous hydroxide formed.

Examples 8, 9 and 10 The following recipe (Table II) was used to prepare three polymers at 5 C. In Example 8 a 1/1 (molar ratio) reaction product of glycidyl methacrylate and'paminodiphenylamine was used as the monomeric anti- The,

' ggaian my roxypmayr me hane-t .fiily nefi txExjample 10 was alcohol coagulatedat 2'4"percen't conver'- sion. Each of the polymerizations was run for 22 hours.

' TABLEII Order tlo'n f Ingredients Water...

Parts 1; Linear dodecyl benzene sullen ate i Sodium salt of condensed naphthalene sulionic acid...

Tripotassium phosphate--.

4o 2 Acrylm'riti-ilo .t-Dodecyl meroa mn Monomeric antioxidant 5 But-adiene-lfl ater 6 Chelating agent 2 7 {FeSO4-7HaO Cumene hydroperoxide See footnote 2, Table I.

Table HI contains oxygen absorption data for the polymers prepared in Examples 3 to 10.

Before oxygen absorption tests were run on the polymers described in Table III, the dry polymers were extracted for 48 hours with methanol 1 in a Soxhlet type apparatus to remove any of the free monomeric age resister and dried. The amount of oxygen absorbed in a particular interval of time was determined for each sample and is listed in the following Table III. An unstabilized NBR rubber would absorb 1 percent 0 at 100 C. in less than 10 hours.

TABLE I11 Oxygen absorption Hours to 1% 0 at 100 C. 293 and 345 385 (to .88% O 264 418 393 410 485 10 410 The above data demonstrate that the monomeric antioxidants described herein are capable of providing age resistant polymeric compositions by either polymerizing the monomeric antioxidants in an emulsion-free radical polymerization system along with comonomers. That is, the age resisters provide protection whether in a free or bound condition. Any of the monomeric antioxidants or polymers described earlier herein can be substituted for their counterparts in the above working examples to provide age resistant polymeric compositions.

NBR and SBR polymers were stabilized by physical incorporation of 1.47 and 1.25 parts respectively of a reaction product of glycidyl methacrylate and p-aminodiphenylamine (1/1 molar ratio). Both polymers were stabilized quite efiectively.

Naturally polymerization rates and amounts of bound Example QQUILU monomer can vary, as well ,as thetypeof emulsifier to be.

I 1 The SBR types were extracted with acetone.

. 12 r t t The age jresistant" polymeric'compositions prepared by chemically binding the'antioxidan'ts: orby physically incorporating them into polymers, are age resistant, whether vulcanized or unvulcanized form. They may be used, depending on the particular polymer-"involved, in products such astirefs, industrial rubber products, such' as transmission belts and hose, and molded goods. Where the vpolymeric composition contains the antioxidant as an integral part of thepolymer chain, it is especially useful in applications where a product i s-frequentlyexposed to aqueous detergent solutions or dry-cleaning fiuids,for' example, in foam backings for rugs and in polymer treated fabrics. 1

While certain representativeembodiments and details have been shown for the purpose of illustrating the'invention, it will be apparent to those skilled in this" art that various changes and inodifications'may be made therein without departing from the spirit or scope, of the inverttion. 7 a f What is claimed is: p I v 1. A processof preparing an age resistant polymeric composition comprising, polymerizing in an emulsion free radical polymerization system, a monomer system containing at least one monomeric antioxidant having the following structural formula:

Ran m, ru-

wherein R is selected from the g roupc onsistiiig of alkyl radicals having 1 to 12 carbon atoms, eycloalkyl radicals having 5 to 12 carbon atoms, aralkylradicalshaving] to 24 carbon atoms'and' aryl radicals having 6' to 24 carbon atoms wherein R fand R are selected fromthe group consisting of hydrogen and alkyl groups having 1 to 4 carbon atoms and wherein R is selected from the group consisting of hydrogen, alkyl radicals having 1 to 12ca rbon atoms, cycloalkylradicals having from 5 to 12',ca rbon atoms, and aralkylradicals having 7 to 24 carbon atoms, wherein R R RF, R and R are selected from the group consisting of hydrogen and alkyl radicals having from 1 to 4 carbon atoms, wherein R 'is selected from the group consisting of hydrogen; alkyl radicals haying from 1 to 4 carbon atoms, carboxymethyl radical: carbalkoxymethyl radicals; and wherein R 9 is selected from the group consisting of hydrogen; alkyl .-radicals having from 1 to 4 carbon atoms, phenyl and substituted phenyl radicals having a substituent selected from the group consisting of alkyl radicals having. 1 m4 carbon atoms and alkoxy radicals having 1 or 2 carbon atoms; .carboxyl radical and carbalkoxy radicals and wherein the :monomer system contains-at least 40 parts byweight of a conjugated diene-1,3 monomer per parts byweight of a conjugated diene-1,3 monomer per'lOO parts by weight of total monomer in the monomer system and 0.10 to 20 parts by weight of the monomeric antioxidant,

2. The process according to claim' 1 wherein the substituted phenyl radicals'p'ossess a substituent selected from the group consisting of alkyl radicals having 1 to 4 car- 4. The process according to claim 1 wherein the monomer system is comprised of from 50 to 99.9 parts of at least one conjugated diene monomer, to 49.9 parts of at least one compound selected from that group consisting of vinyl monomers and vinylidene monomers and 0.10 to 10.0 parts by weight of at least one monomeric antioxidant according to claim 1, all parts being by weight per 100 parts by weight of total monomer.

5. The process according to claim 1 wherein R is selected from the group consisting of hydrogen, methyl, a carboxymethyl radical and carbalkoxymethyl radicals having the following structural formula wherein R is an alkyl radical having from 1 to 4 carbon atoms,, wherein R is selected from the group consisting of hydrogen, phenyl, a carboxyl radical and carbalkoxy radicals having the following structural formula:

wherein R is an alkyl radical having from 1 to 4 carbon atoms.

6. The process according to claim 1 wherein -NHR is in the para position.

7. The process according to claim 1 wherein the sum 14 of the carbon atoms in R and R are 4 or less and wherein the sum of carbon atoms in R and R are 4 or less.

8. The process according to claim 7 wherein R is selected from the group consisting of hydrogen and methyl and R is hydrogen.

9. The process according to claim 5 wherein R and R are selected from the group consisting of methyl and ethyl radicals.

10. The process according to claim 1 wherein the monomeric antioxidant is 3-N-(4-anilinophenyl) amino 2 hydroxypropyl methacrylate.

11. The process according to claim 1 wherein the monomeric antioxidant is a reaction product of glycidyl methacrylate and p-aminodiphenylamine.

References Cited UNITED STATES PATENTS 2,901,502 8/1959 Young et a1 26045.9 3,539,343 11/1970 Munder et a1 96-35.1 3,565,779 2/1971 Luders et al 204-159.14

LESTER L. LEE, Primary Examiner US. Cl. X.R.

26047 R, 62, 83.5, 85.5 ES, 86.1 N, 86.3, 86.7, 482 R, 879

@2 33 UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3, 7 9 Dat.fi June 18, 197

lemme) Carl 'R. Parks It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected ahownbeluwz Column 3, in the formula, between C=O and 3 -0-3 insert (I) Column 6, line #6, "Arak'yl" should read Aralkyl Column 7, line 60, "monomers systems" should read monomer" systems Column 9, line 20, after 'styrfene" place a comma 5' line 33, "omers" should read omer Column 12, line 6% should be deleted.

Signed and sealed this 3rd day of December 1974.

(SEAL) Attest:

McCOY M. GIBSON JR. c. MARSHALL DANN Attesting Officer Comissioner of Patents 

